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Scientific Reports, ISSN 2045-2322, 12/2017, Volume 7, Issue 1, pp. 16275 - 12
While amyloid-beta protein (A beta) aggregation into insoluble plaques is one of the pathological hallmarks of Alzheimer's disease (AD), soluble oligomeric A... 
EFFICACY | AMINO-ACID PEPTIDES | ALZHEIMERS-DISEASE | AMYLOID-BETA | INFLAMMATION | DEPOSITION | MULTIDISCIPLINARY SCIENCES | HYPOTHESIS | DUPLICATION | MOLECULAR-MECHANISMS | Learning | Pathology | Neurodegenerative diseases | Cognition & reasoning | Neurodegeneration | Presenilin 1 | Memory | Amyloid | Cognition | Alzheimer's disease | Plaques | Index Medicus
Journal Article
Ophthalmology, ISSN 0161-6420, 2014, Volume 121, Issue 5, pp. 1045 - 1053
Journal Article
Neurology, ISSN 0028-3878, 03/2012, Volume 78, Issue 10, pp. 690 - 695
Objective: Age at onset of diagnostic motor manifestations in Huntington disease (HD) is strongly correlated with an expanded CAG trinucleotide repeat. The... 
HOMOZYGOSITY | ALLELE | OF-ONSET | GENE | LENGTH | MUTATION | CHROMOSOMES | CLINICAL NEUROLOGY | TRINUCLEOTIDE REPEAT | Humans | Age of Onset | Alleles | Huntington Disease - genetics | Adult | Female | Genotype | Huntington Disease - diagnosis | Male | Trinucleotide Repeat Expansion | Index Medicus | Abridged Index Medicus | 164
Journal Article
Scientific Reports, ISSN 2045-2322, 09/2015, Volume 5, pp. 13222 - 13222
Strong evidence exists for a central role of amyloid beta-protein (A beta) oligomers in the pathogenesis of Alzheimer's disease. We have developed a fast,... 
AMYLOID PEPTIDE | IN-VITRO | A-BETA(1-42) | MULTIDISCIPLINARY SCIENCES | NEURODEGENERATION | IMAGE PHAGE DISPLAY | ALZHEIMERS | AGGREGATION | CELLULAR PRION PROTEIN | TRANSGENIC MICE | IMPAIRMENT | Index Medicus
Journal Article
by Oosterloo, Mayke and Bijlsma, Emilia K and van Kuijk, Sander MJ and Minkels, Floor and de Die-Smulders, Christine EM and Bachoud-Lévi, Anne-Catherine and Bentivoglio, Anna-Rita and Bentivoglio, Anna Rita and Biunno, Ida and Bonelli, Raphael M and Bronzova, Juliana and Burgunder, Jean-Marc and Dunnett, Stephen and Dunnett, Stephen B and Ferreira, Joaquim J and Frich, Jan C and Frich, Jan and Giuliano, Joe and Handley, Olivia J and Heiberg, Arvid and Illarioshkin, Sergey and Illmann, Torsten and Klempir, Jiri and Landwehrmeyer, Bernhard and Landwehrmeyer, G. Bernhard and Levey, Jamie and McLean, Tim and Nielsen, Jørgen and Nielsen, Jørgen E and Koivisto, Susana Pro and Päivärinta, Markku and Pålhagen, Sven and Quarrell, Oliver and Ramos-Arroyo, Maria and Ramos-Arroyo, Maria Antonia and Roos, Raymund A.C and Roos, Raymund AC and Roos, Peter and Saft, Carsten and Sebastián, Ana Rojo and Tabrizi, Sarah and Tabrizi, Sarah J and Vandenberghe, Wim and Verellen-Dumoulin, Christine and Uhrova, Tereza and Wahlström+, Jan and Zaremba, Jacek and (formerly Rödig, Verena Baake and Barth, Katrin and Garde, Monica Bascuñana and Becanovic, Kristina and Bernard, Tomáš and Betz, Sabrina and Bos, Reineke and Come, Adrien and Guedes, Leonor Correia and Callaghan, Jenny and Capodarca, Selene and Charpentier, Sébastien and Vieira da Silva, Wildson and Di Renzo, Martina and Ecker, Daniel and Finisterra, Ana Maria and Fullam, Ruth and Genoves, Camille and Gilling, Mette and Horta, Andrea and Hvalstedt, Carina and Held, Christine and Hussain, Hasina and Koppers, Kerstin and Lamanna, Claudia and Laurà, Matilde and Descals, Asunción Martínez and Martinez-Horta, Saul and Mestre, Tiago and Minster, Sara and Monza, Daniela and Münkel, Kristina and Mütze, Lisanne and Oehmen, Martin and Padieu, Helene and Paterski, Laurent and Peppa, Nadia and Rindal, Beate and Rogers, Dawn and Røren (formerly Heinonen), Niini and Salgueiro, Ana and Šašinková, Pavla and Seliverstov, Yury and Taylor, Catherine and Taylor, Cat and Taylor, Rachel and Taylor, Anne-Marie and Timewell, Erika and Townhill, Jenny and Cubillo, Patricia Trigo and van Walsem, Marleen R and van Walsem, Marleen and Witjes-Ané, Marie-Noelle and ... and EHDN's associate site in Singapore and REGISTRY Investigators of the European Huntington's Disease Network and Registry Steering committee and Language coordinators
Parkinsonism and Related Disorders, ISSN 1353-8020, 04/2019, Volume 61, pp. 101 - 105
The frequency of late-onset Huntington's disease (>59 years) is assumed to be low and the clinical course milder. However, previous literature on late-onset... 
Age of onset | Huntington's disease | Late-onset Huntington's disease | CLINICAL NEUROLOGY | AGE | FEATURES | Genetic research
Journal Article